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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:RAB7A-ATG7

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RAB7A-ATG7
FusionPDB ID: 71472
FusionGDB2.0 ID: 71472
HgeneTgene
Gene symbol

RAB7A

ATG7

Gene ID

7879

10533

Gene nameRAB7A, member RAS oncogene familyautophagy related 7
SynonymsCMT2B|PRO2706|RAB7APG7-LIKE|APG7L|GSA7
Cytomap

3q21.3

3p25.3

Type of geneprotein-codingprotein-coding
Descriptionras-related protein Rab-7aRAB7, member RAS oncogene familyRas-associated protein RAB7ubiquitin-like modifier-activating enzyme ATG7APG7 autophagy 7-likeATG12-activating enzyme E1 ATG7hAGP7ubiquitin-activating enzyme E1-like protein
Modification date2020032820200329
UniProtAcc.

O95352

Ensembl transtripts involved in fusion geneENST idsENST00000265062, ENST00000482525, 
ENST00000485280, 
ENST00000469654, 
ENST00000354449, ENST00000446450, 
ENST00000354956, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score21 X 11 X 12=277212 X 13 X 12=1872
# samples 2321
** MAII scorelog2(23/2772*10)=-3.59122149119284
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(21/1872*10)=-3.15611920191728
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RAB7A [Title/Abstract] AND ATG7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RAB7A(128526514)-ATG7(11596285), # samples:1
Anticipated loss of major functional domain due to fusion event.RAB7A-ATG7 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RAB7A-ATG7 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RAB7A-ATG7 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
RAB7A-ATG7 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
RAB7A-ATG7 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
RAB7A-ATG7 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneRAB7A

GO:0022615

protein to membrane docking

24344282

TgeneATG7

GO:0006497

protein lipidation

12890687

TgeneATG7

GO:0009267

cellular response to starvation

20543840

TgeneATG7

GO:0031401

positive regulation of protein modification process

12890687

TgeneATG7

GO:0071455

cellular response to hyperoxia

20543840


check buttonFusion gene breakpoints across RAB7A (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across ATG7 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-CD-8534-01ARAB7Achr3

128526514

+ATG7chr3

11596285

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000265062RAB7Achr3128526514+ENST00000354956ATG7chr311596285+1047774246806186
ENST00000482525RAB7Achr3128526514+ENST00000354956ATG7chr311596285+835562774340144

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000265062ENST00000354956RAB7Achr3128526514+ATG7chr311596285+0.0018021750.99819785
ENST00000482525ENST00000354956RAB7Achr3128526514+ATG7chr311596285+0.0058681830.99413186

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>71472_71472_1_RAB7A-ATG7_RAB7A_chr3_128526514_ENST00000265062_ATG7_chr3_11596285_ENST00000354956_length(amino acids)=186AA_BP=
MTSRKKVLLKVIILGDSGVGKTSLMNQYVNKKFSNQYKATIGADFLTKEVMVDDRLVTMQIWDTAGQERFQSLGVAFYRGADCCVLVFDV
TAPNTFKTLDSWRDEFLIQASPRDPENFPFVVLGNKIDLENRQVATKRAQAWCYSKNNIPYFETSAKEAINVEQAFQTIARNALKQIWDM

--------------------------------------------------------------

>71472_71472_2_RAB7A-ATG7_RAB7A_chr3_128526514_ENST00000482525_ATG7_chr3_11596285_ENST00000354956_length(amino acids)=144AA_BP=1
MNPEQRRTLATPGQQRGESQTSGYGGGAQNHQAWGQQSCSGDGELLSRRPGRSQPHSGAISDGLIIAHVPDLLKCIPCNRLERLLHVDGL

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr3:128526514/chr3:11596285)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.ATG7

O95352

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: E1-like activating enzyme involved in the 2 ubiquitin-like systems required for cytoplasm to vacuole transport (Cvt) and autophagy. Activates ATG12 for its conjugation with ATG5 as well as the ATG8 family proteins for their conjugation with phosphatidylethanolamine. Both systems are needed for the ATG8 association to Cvt vesicles and autophagosomes membranes. Required for autophagic death induced by caspase-8 inhibition. Required for mitophagy which contributes to regulate mitochondrial quantity and quality by eliminating the mitochondria to a basal level to fulfill cellular energy requirements and preventing excess ROS production. Modulates p53/TP53 activity to regulate cell cycle and survival during metabolic stress. Plays also a key role in the maintenance of axonal homeostasis, the prevention of axonal degeneration, the maintenance of hematopoietic stem cells, the formation of Paneth cell granules, as well as in adipose differentiation. Plays a role in regulating the liver clock and glucose metabolism by mediating the autophagic degradation of CRY1 (clock repressor) in a time-dependent manner (By similarity). {ECO:0000250|UniProtKB:Q9D906, ECO:0000269|PubMed:11096062, ECO:0000269|PubMed:16303767, ECO:0000269|PubMed:22170151}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRAB7Achr3:128526514chr3:11596285ENST00000265062+5637_45176.0208.0MotifEffector region
HgeneRAB7Achr3:128526514chr3:11596285ENST00000265062+56125_128176.0208.0Nucleotide bindingGTP
HgeneRAB7Achr3:128526514chr3:11596285ENST00000265062+56156_157176.0208.0Nucleotide bindingGTP
HgeneRAB7Achr3:128526514chr3:11596285ENST00000265062+5615_22176.0208.0Nucleotide bindingGTP
HgeneRAB7Achr3:128526514chr3:11596285ENST00000265062+5634_40176.0208.0Nucleotide bindingGTP
HgeneRAB7Achr3:128526514chr3:11596285ENST00000265062+5663_67176.0208.0Nucleotide bindingGTP

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneATG7chr3:128526514chr3:11596285ENST00000354449171915_17693.0704.0MotifNote=FAP motif
TgeneATG7chr3:128526514chr3:11596285ENST00000354956161815_17666.0677.0MotifNote=FAP motif
TgeneATG7chr3:128526514chr3:11596285ENST00000446450151715_17613.0624.0MotifNote=FAP motif


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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RAB7A
ATG7


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to RAB7A-ATG7


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to RAB7A-ATG7


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource